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Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Recalled February 5, 2020 · FDA recall Z-0919-2020 · Arthrex
Hazard
There is a potential for blockage of the Hub Attachment Tube. · FDA Class II
Units
47
Sold at
Nationwide in US; no distribution OUS.
Description
There is a potential for blockage of the Hub Attachment Tube.
Product
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Manufacturer(s)
Arthrex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →